K-number	K063355
Device name	D-LINE CATHETER ST, DOUBLE LUMEN ST; EXTRA FLOW
Applicant	Novosci Corp.
Product code	MPB
Device class	Class II
Decision date	Jul 27, 2007
Decision	Unknown
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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D-LINE CATHETER ST, DOUBLE LUMEN ST; EXTRA FLOW

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